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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499248Generated: October 27, 2026

Oxalyl chloride → 4-(2-Fluorophenyl)-6-methyl-2-morpholin-4-yl-pyrimidine-5-carboxylic acid benzyl-isopropyl-amide

https://huagongshe.com/reaction/499248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantIsopropylbenzylamineHCID 66024—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(2-Fluorophenyl)-6-methyl-2-morpholin-4-yl-pyrimidine-5-carboxylic acidHCID 59421180—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(2-Fluorophenyl)-6-methyl-2-morpholin-4-yl-pyrimidine-5-carboxylic acid benzyl-isopropyl-amideHCID 1160479340%

Reaction Steps

A solution of 2 M oxalyl chloride in CH2Cl2 (0.070 mL, 0.14 mmol) was added to a stirred solution of 4-(2-fluorophenyl)-6-methyl-2-morpholin-4-yl-pyrimidine-5-carboxylic acid (0.03 g, 0.09 mmol) in CH2Cl2 (2 mL) and DMF (0.030 mL) at room temperature, and stirring continued for 15 min. A solution of N-benzylisopropylamine (0.013 g, 0.1 mmol) in CH2Cl2(1 mL) and diisopropylethylamine(0.044 mL,0.25 mmol) were added and stirred for 24 hr. The solvent was removed under reduced pressure, and the residue was purified by Biotage SP1 on packed silica gel column (10%-80% EtOAc/Hexanes gradient) to give 4-(2-fluorophenyl)-6-methyl-2-morpholin-4-yl-pyrimidine-5-carboxylic acid benzyl-isopropyl-amide (0.016 g,40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767680B2
Source datasetuspto-grants-2010_08
ORD IDord-3211c72a54f04400921535ebc5708bda
Source noteuspto-grants-2010_08